Long-term prognosis and transition period until progression in fibrotic hypersensitivity pneumonitis
Nearly half of fHP patients progressed to PPF within a few years, with markedly reduced survival. Early recognition of high-risk patients may support timely anti-fibrotic treatment and improve outcomes.
Authors
- María Florencia Pilia (ORCID: https://orcid.org/0009-0003-2880-4019)
- Anna Maria Villar (ORCID: https://orcid.org/0000-0002-5106-8334)
- I Ojanguren
- Xavier Muñoz
- Irene Sansano
- David Espejo
- María Jesú Cruz
- Chirstian Romero
- Antia Ferreiro-Posse
- Marta Andreu-Casas
Publication Details
- Journal
- Respiration
- Published
- 2026-03-05
- DOI
- https://doi.org/10.1159/000551084
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00